돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 324861생성일: 2026년 10월 26일

Triethylamine → Diethyl 2,6-diisopropyl-4-[(2-trimethylsilylethynyl)phenyl]pyridine-3,5-dicarboxylate

https://huagongshe.com/reaction/324861

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물TriphenylphosphineHCID 11776—
반응물TrimethylsilylacetyleneHCID 66111—
반응물Diethyl 2,6-diisopropyl-4-(2-iodophenyl)pyridine-3,5-dicarboxylateHCID 22005000—
촉매Copper iodideHCID 83717—
촉매Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
용매TolueneHCID 1140—
생성물Diethyl 2,6-diisopropyl-4-[(2-trimethylsilylethynyl)phenyl]pyridine-3,5-dicarboxylateHCID 2200512783.3%

반응 단계

A solution of 1.50 g (3 mmole) of the intermediate obtained in Step A in toluene was treated with 1.48 g (15 mmole) of trimethylsilyl acetylene, 87.1 g (0.86 mol) of triethylamine, 0.1 g (0.15 mmol) of bis(triphenylphosphine) palladium(II) chloride, 0.2 g (0.8 mmole) of triphenyl phosphine and 0.2 g (1.17 mmole) of copper iodide. This reaction mixture was stirred at rt for 1 hr and heated at 90° C., in a sealed reaction vessel, for 16 hrs. The reaction mixture was to cooled to temperature, filtered through Celite, and stripped to give a dark oil which upon purification by flash silica gel chromatography to yield 1.22 g (2.5 mmole) of the product. 1H NMR (300 MHz, CDCl3): δ 0.0 (s, 9 H), 0.93 (t, J=7.0, 61), 1.32 (d, J=6.6 Hz, 6 H), 1.33 (d, J=6.6 Hz, 6 H), 3.18 (septet, J=6.6, 2 H), 3.90 (q, J=7.0 Hz, 4 H), 7.20-7.50 (m, 4 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06218431B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-2047284ce66a4eb491d40b169aa2e5d1
출처 메모uspto-grants-2001_04